ALOMONE LABS Non-Antibody Products — page 10 of 36
Non-Antibody Products
Page 10 of 36
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| CyPPA | CyPPA is an activator of small conductance Ca2+-activated K+ channels KCa2… | 10 mg | C-110 | More Info |
| CyPPA | CyPPA is an activator of small conductance Ca2+-activated K+ channels KCa2… | 25 mg | C-110 | More Info |
| CyPPA | CyPPA is an activator of small conductance Ca2+-activated K+ channels KCa2… | 5 mg | C-110 | More Info |
| CyPPA | CyPPA is an activator of small conductance Ca2+-activated K+ channels KCa2… | 50 mg | C-110 | More Info |
| (-)-Cytisine | (-)-Cytisine is a potent and selective agonist of neuronal nAChR. It acts… | 10 mg | C-130 | More Info |
| (-)-Cytisine | (-)-Cytisine is a potent and selective agonist of neuronal nAChR. It acts… | 100 mg | C-130 | More Info |
| (-)-Cytisine | (-)-Cytisine is a potent and selective agonist of neuronal nAChR. It acts… | 25 mg | C-130 | More Info |
| (-)-Cytisine | (-)-Cytisine is a potent and selective agonist of neuronal nAChR. It acts… | 250 mg | C-130 | More Info |
| (-)-Cytisine | (-)-Cytisine is a potent and selective agonist of neuronal nAChR. It acts… | 50 mg | C-130 | More Info |
| Cytochalasin E | Cytochalasin E is a fungal toxin which inhibits actin polymerization and b… | 5 x 1 mg | C-550 | More Info |
| Cytochalasin E | Cytochalasin E is a fungal toxin which inhibits actin polymerization and b… | 1 mg | C-550 | More Info |
| [D-Ala7]-Angiotensin I/II (1-7) | An Angiotensin (1-7) Antagonist1. Synthetic peptide. Purity ≥98% (HPLC)… | 1 mg | SPA-160 | More Info |
| [D-Ala7]-Angiotensin I/II (1-7) | An Angiotensin (1-7) Antagonist1. Synthetic peptide. Purity ≥98% (HPLC)… | 10 mg | SPA-160 | More Info |
| [D-Ala7]-Angiotensin I/II (1-7) | An Angiotensin (1-7) Antagonist1. Synthetic peptide. Purity ≥98% (HPLC)… | 100 mg | SPA-160 | More Info |
| [D-Ala7]-Angiotensin I/II (1-7) | An Angiotensin (1-7) Antagonist1. Synthetic peptide. Purity ≥98% (HPLC)… | 25 mg | SPA-160 | More Info |
| [D-Ala7]-Angiotensin I/II (1-7) | An Angiotensin (1-7) Antagonist1. Synthetic peptide. Purity ≥98% (HPLC)… | 5 mg | SPA-160 | More Info |
| [D-Ala7]-Angiotensin I/II (1-7) | An Angiotensin (1-7) Antagonist1. Synthetic peptide. Purity ≥98% (HPLC)… | 50 mg | SPA-160 | More Info |
| Dantrolene sodium salt | RYR antagonist. Purity ≥99%. MW: 336.23 | 5 mg | D-185 | More Info |
| D-AP5 | D-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &m… | 1 mg | D-145 | More Info |
| D-AP5 | D-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &m… | 10 mg | D-145 | More Info |
| D-AP5 | D-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &m… | 100 mg | D-145 | More Info |
| D-AP5 | D-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &m… | 25 mg | D-145 | More Info |
| D-AP5 | D-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &m… | 250 mg | D-145 | More Info |
| D-AP5 | D-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &m… | 5 mg | D-145 | More Info |
| D-AP5 | D-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &m… | 50 mg | D-145 | More Info |
| D-AP5 | D-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &m… | 500 mg | D-145 | More Info |
| Dapoxetine hydrochloride | Dapoxetine blocks with an IC50 of 5.3 µM for cloned KV4.3 and 11.6 &… | 10 mg | D-175 | More Info |
| Dapoxetine hydrochloride | Dapoxetine blocks with an IC50 of 5.3 µM for cloned KV4.3 and 11.6 &… | 100 mg | D-175 | More Info |
| Dapoxetine hydrochloride | Dapoxetine blocks with an IC50 of 5.3 µM for cloned KV4.3 and 11.6 &… | 25 mg | D-175 | More Info |
| Dapoxetine hydrochloride | Dapoxetine blocks with an IC50 of 5.3 µM for cloned KV4.3 and 11.6 &… | 50 mg | D-175 | More Info |
| Darusentan | Darusentan is a selective antagonist of ET-A Endothelin receptors, inhibit… | 10 mg | D-265 | More Info |
| Darusentan | Darusentan is a selective antagonist of ET-A Endothelin receptors, inhibit… | 25 mg | D-265 | More Info |
| Darusentan | Darusentan is a selective antagonist of ET-A Endothelin receptors, inhibit… | 5 mg | D-265 | More Info |
| Darusentan | Darusentan is a selective antagonist of ET-A Endothelin receptors, inhibit… | 50 mg | D-265 | More Info |
| δ-Dendrotoxin | δ-Dendrotoxin inhibits 4-AP sensitive, inactivating voltage-gated K+… | 0.5 mg | D-380 | More Info |
| δ-Dendrotoxin | δ-Dendrotoxin inhibits 4-AP sensitive, inactivating voltage-gated K+… | 1 mg | D-380 | More Info |
| δ-Dendrotoxin | δ-Dendrotoxin inhibits 4-AP sensitive, inactivating voltage-gated K+… | 5 mg | D-380 | More Info |
| δ-Dendrotoxin | δ-Dendrotoxin inhibits 4-AP sensitive, inactivating voltage-gated K+… | 70 µg | D-380 | More Info |
| δ-Dendrotoxin | δ-Dendrotoxin inhibits 4-AP sensitive, inactivating voltage-gated K+… | 70 µg - Free Sample | D-380 | More Info |
| Dendrotoxin-I | Dendrotoxin-I is a highly selective blocker of voltage-gated K+ channels (… | 0.1 mg | D-390 | More Info |
| Dendrotoxin-I | Dendrotoxin-I is a highly selective blocker of voltage-gated K+ channels (… | 0.14 mg | D-390 | More Info |
| Dendrotoxin-I | Dendrotoxin-I is a highly selective blocker of voltage-gated K+ channels (… | 5 x 0.14 mg | D-390 | More Info |
| Dendrotoxin-I | Dendrotoxin-I is a highly selective blocker of voltage-gated K+ channels (… | 50 µg | D-390 | More Info |
| Dendrotoxin-K | Dendrotoxin-K is a highly selective blocker of voltage-gated K+ channels (… | 10 µg | D-400 | More Info |
| Dendrotoxin-K | Dendrotoxin-K is a highly selective blocker of voltage-gated K+ channels (… | 70 µg | D-400 | More Info |
| D-3263 hydrochloride | D-3263 hydrochloride is a potent TRPM8 channel agonist1.It shows evidence… | 10 mg | D-195 | More Info |
| D-3263 hydrochloride | D-3263 hydrochloride is a potent TRPM8 channel agonist1.It shows evidence… | 25 mg | D-195 | More Info |
| D-3263 hydrochloride | D-3263 hydrochloride is a potent TRPM8 channel agonist1.It shows evidence… | 5 mg | D-195 | More Info |
| D-3263 hydrochloride | D-3263 hydrochloride is a potent TRPM8 channel agonist1.It shows evidence… | 50 mg | D-195 | More Info |
| Diazepam | Diazepam is a positive allosteric modulator of GABAA receptors at the benz… | 1 g | D-215 | More Info |
| Diazepam | Diazepam is a positive allosteric modulator of GABAA receptors at the benz… | 100 mg | D-215 | More Info |
| Diazepam | Diazepam is a positive allosteric modulator of GABAA receptors at the benz… | 250 mg | D-215 | More Info |
| Diazepam | Diazepam is a positive allosteric modulator of GABAA receptors at the benz… | 50 mg | D-215 | More Info |
| 5,7-Dichlorokynurenic acid | 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… | 10 mg | D-190 | More Info |
| 5,7-Dichlorokynurenic acid | 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… | 100 mg | D-190 | More Info |
| 5,7-Dichlorokynurenic acid | 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… | 25 mg | D-190 | More Info |
| 5,7-Dichlorokynurenic acid | 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… | 50 mg | D-190 | More Info |
| 5,7-Dichlorokynurenic acid monohydrate | 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… | 10 mg | D-191 | More Info |
| 5,7-Dichlorokynurenic acid monohydrate | 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… | 100 mg | D-191 | More Info |
| 5,7-Dichlorokynurenic acid monohydrate | 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… | 25 mg | D-191 | More Info |
| 5,7-Dichlorokynurenic acid monohydrate | 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… | 250 mg | D-191 | More Info |
| 5,7-Dichlorokynurenic acid monohydrate | 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the gl… | 50 mg | D-191 | More Info |
| Diclofenac | Diclofenac is a KCNQ opener with anti-nociceptive properties1. Synthetic.… | 1 g | D-180 | More Info |
| Diclofenac | Diclofenac is a KCNQ opener with anti-nociceptive properties1. Synthetic.… | 10 g | D-180 | More Info |
| Diclofenac | Diclofenac is a KCNQ opener with anti-nociceptive properties1. Synthetic.… | 25 g | D-180 | More Info |
| Diclofenac | Diclofenac is a KCNQ opener with anti-nociceptive properties1. Synthetic.… | 5 g | D-180 | More Info |
| Diclofenac sodium salt | Diclofenac is a KCNQ opener with anti-nociceptive properties1. Synthetic.… | 25 g | D-181 | More Info |
| Diclofenac sodium salt | Diclofenac is a KCNQ opener with anti-nociceptive properties1. Synthetic.… | 5 g | D-181 | More Info |
| Diclofenac sodium salt | Diclofenac is a KCNQ opener with anti-nociceptive properties1. Synthetic.… | 50 g | D-181 | More Info |
| Diltiazem hydrochloride | IC50 was 33 µM on CaV1.2 channels in expression systems1. Synthetic.… | 1 g | D-135 | More Info |
| Diltiazem hydrochloride | IC50 was 33 µM on CaV1.2 channels in expression systems1. Synthetic.… | 10 g | D-135 | More Info |
| Diltiazem hydrochloride | IC50 was 33 µM on CaV1.2 channels in expression systems1. Synthetic.… | 5 g | D-135 | More Info |
| 2,5-dimethylcelecoxib | 2,5-dimethylcelecoxib is a KCNQ channel opener in smooth muscle cells1. Sy… | 10 mg | D-150 | More Info |
| 2,5-dimethylcelecoxib | 2,5-dimethylcelecoxib is a KCNQ channel opener in smooth muscle cells1. Sy… | 25 mg | D-150 | More Info |
| 2,5-dimethylcelecoxib | 2,5-dimethylcelecoxib is a KCNQ channel opener in smooth muscle cells1. Sy… | 5 mg | D-150 | More Info |
| 2,5-dimethylcelecoxib | 2,5-dimethylcelecoxib is a KCNQ channel opener in smooth muscle cells1. Sy… | 50 mg | D-150 | More Info |
| 1,1-Dimethyl-4-phenylpiperazinium iodide | DMPP activates α4 nicotinic channels expressed in Xenopus oocytes wi… | 1 g | D-125 | More Info |
| 1,1-Dimethyl-4-phenylpiperazinium iodide | DMPP activates α4 nicotinic channels expressed in Xenopus oocytes wi… | 10 g | D-125 | More Info |
| 1,1-Dimethyl-4-phenylpiperazinium iodide | DMPP activates α4 nicotinic channels expressed in Xenopus oocytes wi… | 5 g | D-125 | More Info |
| D-IP3 | IP3 Receptor agonist (active analogue). Purity ≥99%. MW: 420.09 | 0.1 mg | D-220 | More Info |
| DL-AP3 | DL-AP3 is a selective competitive antagonist of group I metabotropic gluta… | 100 mg | D-275 | More Info |
| DL-AP3 | DL-AP3 is a selective competitive antagonist of group I metabotropic gluta… | 250 mg | D-275 | More Info |
| DL-AP3 | DL-AP3 is a selective competitive antagonist of group I metabotropic gluta… | 50 mg | D-275 | More Info |
| DL-AP3 | DL-AP3 is a selective competitive antagonist of group I metabotropic gluta… | 500 mg | D-275 | More Info |
| DL-AP5 | DL-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &… | 10 mg | D-140 | More Info |
| DL-AP5 | DL-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &… | 100 mg | D-140 | More Info |
| DL-AP5 | DL-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &… | 25 mg | D-140 | More Info |
| DL-AP5 | DL-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &… | 5 mg | D-140 | More Info |
| DL-AP5 | DL-AP5 is an NMDA receptor antagonist. IC50 = 0.28 µM (NR2A), 0.46 &… | 50 mg | D-140 | More Info |
| DL-AP7 | DL-AP7 is an NMDA receptor antagonist1. Synthetic. Purity >99%. MW: 225.19 | 10 mg | D-200 | More Info |
| DL-AP7 | DL-AP7 is an NMDA receptor antagonist1. Synthetic. Purity >99%. MW: 225.19 | 25 mg | D-200 | More Info |
| DL-AP7 | DL-AP7 is an NMDA receptor antagonist1. Synthetic. Purity >99%. MW: 225.19 | 5 mg | D-200 | More Info |
| DL-AP7 | DL-AP7 is an NMDA receptor antagonist1. Synthetic. Purity >99%. MW: 225.19 | 50 mg | D-200 | More Info |
| DMAB-anabaseine dihydrochloride | DMAB-anabaseine dihydrochloride is a partial agonist of α7 nicotinic… | 1 g | D-110 | More Info |
| DMAB-anabaseine dihydrochloride | DMAB-anabaseine dihydrochloride is a partial agonist of α7 nicotinic… | 10 g | D-110 | More Info |
| DMAB-anabaseine dihydrochloride | DMAB-anabaseine dihydrochloride is a partial agonist of α7 nicotinic… | 10 mg | D-110 | More Info |
| DMAB-anabaseine dihydrochloride | DMAB-anabaseine dihydrochloride is a partial agonist of α7 nicotinic… | 5 g | D-110 | More Info |
| DMAB-anabaseine dihydrochloride | DMAB-anabaseine dihydrochloride is a partial agonist of α7 nicotinic… | 5 mg | D-110 | More Info |
| DMAB-anabaseine dihydrochloride | DMAB-anabaseine dihydrochloride is a partial agonist of α7 nicotinic… | 50 mg | D-110 | More Info |
| DM-PPP | DM-PPP is a selective and non-competitive antagonist of mGluR1 receptors.… | 10 mg | D-255 | More Info |
ALOMONE LABS
ALOMONE LABS
Jerusalem BioPark (JBP), Hadassah Ein Kerem
PO Box 4287
Jerusalem, 9104201 ISRAEL
P: +972-2-587-2202
F: +972-2-587-1101
info@alomone.com
http://www.alomone.com
U.S.A. OFFICE
Toll free phone: 1800-618-1644 / 1800-791-3904
Toll free fax: 1888-454-7276 / 1800-791-3912
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